FDA Inspection 593470 — Vitalant

Vitalant — FEI 3003603163

The FDA completed an inspection of Vitalant on Jun 29, 2009 in Villa Park, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 29, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Villa Park, IL (United States)